June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Identification of Novel PIKFYVE Gene Mutations Associated with Fleck Corneal Dystrophy
Author Affiliations & Notes
  • Jessica Gee
    Ophthalmology, Jules Stein Eye Institute - UCLA, Los Angeles, CA
  • Chulaluck Tangmonkongvoragul
    Ophthalmology, Jules Stein Eye Institute - UCLA, Los Angeles, CA
  • Ricardo F Frausto
    Ophthalmology, Jules Stein Eye Institute - UCLA, Los Angeles, CA
  • Doug Chung
    Ophthalmology, Jules Stein Eye Institute - UCLA, Los Angeles, CA
  • Anthony J Aldave
    Ophthalmology, Jules Stein Eye Institute - UCLA, Los Angeles, CA
  • Footnotes
    Commercial Relationships Jessica Gee, None; Chulaluck Tangmonkongvoragul, None; Ricardo Frausto, None; Doug Chung, None; Anthony Aldave, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 2516. doi:
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      Jessica Gee, Chulaluck Tangmonkongvoragul, Ricardo F Frausto, Doug Chung, Anthony J Aldave; Identification of Novel PIKFYVE Gene Mutations Associated with Fleck Corneal Dystrophy. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):2516.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To report two novel mutations in the PIKFYVE gene, one frameshift and the other an interstitial deletion, associated with fleck corneal dystrophy (FCD) in two previously unreported individuals.

Methods: A slit-lamp examination was performed prior to the collection of a saliva sample as a source of genomic DNA. Following DNA extraction, PCR amplification and automated sequencing of all 41 exons of PIKFYVE was performed. Copy number variation (CNV) detection was performed using quantitative PCR (qPCR).

Results: Numerous, panstromal, grayish-white, punctate opacities were observed in both corneas of each individual, consistent with the diagnosis of FCD. Screening of PIKFYVE in the first proband demonstrated a novel heterozygous frameshift mutation in exon 19, c.3151dupA, which is predicted to encode for a truncated PIKFYVE protein, p.(Asp1052Argfs*18). Sanger sequencing of all exons and exon-intron boundaries of PIKFYVE in the second proband did not demonstrate a presumed pathogenic variant. However, qPCR revealed a novel heterozygous deletion involving exon 16[AA1] . Deletions involving PIKFYVE have been reported at a population frequency of 0.000105 (Database of Genomic Variation).<br /> <br />

Conclusions: We report two novel PIKFYVE mutations associated with FCD: a heterozygous frameshift mutation (c.3151dupA), which is only the sixth frameshift mutation associated with FCD; and a heterozygous deletion, which is the first CNV associated with FCD.

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